Structure Information
Structure

Compound Identification

SMILES

CN1CC[NH+](CC2=C([O-])C(C[NH+]3CCN(C)CC3)=C3OC=C(C(=O)C3=C2[O-])C2=CC=C(OC3OC(CO)C(O)C(O)C3O)C=C2)CC1

InChIKey

InChIKey=OFKXUVPCDIHNPX-UHFFFAOYSA-N

Formula

C33H44N4O10

Mass

656.733

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Isoflavonoids

Subclass

Isoflavonoid O-glycosides

Intermediate Tree Nodes

Not available

Direct Parent

Isoflavonoid O-glycosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Isoflavonoid-4p-o-glycoside - Isoflavonoid o-glycoside - Isoflavone - Phenolic glycoside - Fatty acyl glycoside of mono- or disaccharide - Fatty acyl glycoside - Alkyl glycoside - Hexose monosaccharide - O-glycosyl compound - Chromone - Glycosyl compound - Benzopyran - 1-benzopyran - Phenoxy compound - Phenol ether - Aralkylamine - N-alkylpiperazine - Phenoxide - N-methylpiperazine - Pyranone - Monosaccharide - Benzenoid - Oxane - Pyran - Fatty acyl - 1,4-diazinane - Monocyclic benzene moiety - Piperazine - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Polyol - Acetal - Oxacycle - Azacycle - Organoheterocyclic compound - Organooxygen compound - Alcohol - Organic salt - Organic zwitterion - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Organic nitrogen compound - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as isoflavonoid o-glycosides. These are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one.

External Descriptors

Not available

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